Mumbai-based drugmaker BDR Pharmaceuticals has sought the drug controller’s approval to manufacture and sell a generic version of remdesivir without entering into a licensing pact with Gilead Sciences (Nasdaq: GILD), prompting the patent-holder to flag its concerns with the government.
Gilead’s patents on remdesivir in India are valid until 2035 and allow it to exclusively make and sell the drug in the country.
BDR Pharma has requested the Indian drug regulators to expedite manufacturing and marketing license process of remdesivir, a potential drug for COVID-19 treatment.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze